Canonical Allele Identifier: CA556484146

Gene: AGA

Linked Data

• dbSNP Id: rs1202545269
• gnomAD v2: 4-178359851-C-T
• gnomAD v3: 4-177438697-C-T
• gnomAD v4: 4-177438697-C-T
• MyVariant Identifiers: chr4:g.178359851C>T (hg19) ; chr4:g.177438697C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177438697C>T , CM000666.2:g.177438697C>T	GRCh38
NC_000004.11:g.178359851C>T , CM000666.1:g.178359851C>T	GRCh37
NC_000004.10:g.178596845C>T	NCBI36
NG_011845.2:g.8807G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.507+48G>A MANE Select	ENSP00000264595.2:n.507+48G>A
ENST00000264595.6:c.507+48G>A	ENSP00000264595.2:n.507+48G>A
ENST00000502310.5:c.162+48G>A	ENSP00000423798.1:n.162+48G>A
ENST00000506853.5:n.541+48G>A
ENST00000510635.1:c.203+48G>A
ENST00000510955.5:n.428+48G>A
NM_000027.3:c.507+48G>A	NP_000018.2:n.507+48G>A
NM_001171988.1:c.507+48G>A	NP_001165459.1:n.507+48G>A
NR_033655.1:n.635+48G>A
XM_006714123.2:c.507+48G>A	XP_006714186.1:n.507+48G>A
XR_001741155.2:n.601+48G>A
NM_000027.4:c.507+48G>A MANE Select	NP_000018.2:n.507+48G>A
NM_001171988.2:c.507+48G>A	NP_001165459.1:n.507+48G>A
NR_033655.2:n.569+48G>A